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Use of the low-dose corticotropin stimulation test for the monitoring of children with asthma treated with inhaled corticosteroids.

机译:使用小剂量促肾上腺皮质激素刺激试验监测吸入性糖皮质激素治疗的哮喘患儿。

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OBJECTIVE: Subnormal hypothalamic-pituitary-adrenal (HPA) function and rare cases of adrenal crisis have been reported in asthmatic children treated with inhaled corticosteroids. We investigated subnormal HPA activity and followed up affected patients until recovery of normal HPA functions. STUDY DESIGN: 100 children with persistent asthma underwent low-dose corticotropin testing, with the administration of 1 microg of 1-24 ACTH intravenously. Treatments were beclomethasone dipropionate as a metered-dose inhaler, n = 14, budesonide as a dry-powder inhaler, n = 16, fluticasone propionate as a metered-dose inhaler n = 31 or a dry-powder inhaler n = 39. The mean commercially labelled dose was 520 +/- 29 microg/day (mean +/- SEM, range: 160-1,000) and the equipotent dose (which compares the efficiency of these drugs for treating asthma and their responsibility for systemic effects) was 890 +/- 55 microg/day (range: 200-2,000). RESULTS: The mean stimulated cortisol level +/- SEM (and range) of the patient was 482 +/- 12 (148-801), and that of 40 age-matched controls was 580 +/- 12.5 (439-726), (SD = 79). The result was subnormal (more than 2 SD below the mean of the controls) in28 of the 100 patients. One-four stepwise decreases of 10-100% in the daily equipotent doses received by the patients with abnormal low-dose corticotropin testing results led to normal results in subsequent low-dose corticotropin testing in 27 retested patients. The mean time interval between two tests was 5 months (range: 2-6 months) and the mean period required for normalization of the test was 13 months (range: 2-21). Only one case of asthma exacerbation and no adrenal crisis were observed over these periods. CONCLUSIONS: Decreasing daily equipotent doses led to recovery of normal HPA function without asthma exacerbation. Thus, a revision of the doses of inhaled corticosteroids used in asthmatic children with a progressive decrease to the consensus-recommended doses should decrease the systemic effects of inhaled corticosteroids, while minimizing the risk of asthma exacerbation.
机译:目的:报道了接受吸入糖皮质激素治疗的哮喘儿童的下丘脑-垂体-肾上腺(HPA)功能不正常和少见的肾上腺疾病。我们调查了HPA活性低于正常水平并随访受影响的患者,直到HPA功能恢复正常。研究设计:100例患有持续性哮喘的儿童接受了小剂量的促肾上腺皮质激素测试,静脉注射1微克1-24 ACTH。治疗方法为倍丙米氯倍松松作为定量吸入器,n = 14,布地奈德作为干粉吸入器,n = 16,丙酸氟替卡松作为定量吸入器,n = 31或干粉吸入器,n =39。平均值商业标记的剂量为520 +/- 29微克/天(平均+/- SEM,范围:160-1,000),等效剂量(比较这些药物治疗哮喘的效率及其对全身作用的责任)为890 + /-55微克/天(范围:200-2,000)。结果:患者的平均皮质醇刺激水平+/- SEM(和范围)为482 +/- 12(148-801),而40位年龄相匹配的对照组的平均刺激水平为580 +/- 12.5(439-726), (SD = 79)。在100例患者中,有28例结果低于正常水平(比对照组平均值低2 SD)。低剂量促肾上腺皮质激素检测结果异常的患者每日当量剂量的四分之一逐步降低10-100%,导致随后的27例接受再检测的患者进行低剂量促肾上腺皮质激素检测的结果正常。两次测试之间的平均时间间隔为5个月(范围:2-6个月),测试标准化所需的平均时间为13个月(范围:2-21)。在此期间,仅观察到一例哮喘加重且未发生肾上腺危机。结论:减少每日等效剂量可恢复正常的HPA功能,而不会加剧哮喘。因此,将哮喘儿童吸入皮质类固醇的剂量调整为逐步降低至共识推荐剂量应可降低吸入皮质类固醇的全身作用,同时最大程度降低哮喘加重的风险。

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